日本金属学会誌

J. Japan Inst. Metals, Vol. 54, No. 8 (1990),
pp. 870-877

Formation of Austenite and Martensite in the Surface Layer of Pure Iron due to Ion-Nitriding Hardening

Naoki Yasumaru1

1Fukui National College of Technology, Sabae

Abstract:

Pure iron was ion-nitrided in a mixed gas (80 vol% N2+20 vol% H2) under a reduced pressure of 665 Pa at 803, 923 and 1013 K and then quenched in water for the elucidation of the ion-nitriding behaviour accompanied with phase transformations above the eutedoid transformation temperature of 863 K for the Fe-N system.
When nitrided at 803 K, the nitrided case consists of two layers as usual nitrided cases do; (i) a compound layer with a hardness of about Hv 700 which is mainly composed of γ '-Fe4N, and (ii) a diffusion layer of about Hv 250.
When nitrided at 923 K, the nitrided case consists of; (i) a compound layer of about Hv 750, mainly composed of γ '-Fe4N, under which are (ii) an inner layer of γ austenite of about Hv 400 and (iii) a diffusion layer.
When nitrided at 1013 K, the nitrided case consists of; (i) a thin compound layer, (ii) an inner hardened layer of γ and α ' martensite, of which the hardness increases from Hv 400 to Hv 700 toward the inside corresponding to the content of the α ' phase, and (iii) a diffusion layer.
To explain the formation of the relatively thick hardened layers of austenite at 923 K and martensite at 1013 K, the nitrogen concentration at each temperature and the degree of the stability of the γ phase when quenched in water after nitriding were examined.


(Received 1990/1/25)

Keywords:

ion-nitriding, pure iron, nitrided case, phase transformation, austenite, martensite, compound layer, diffusion layer


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